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510(k) FDA Premarket Notification P110042

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The following data is part of a premarket notification filed by with the FDA for .

Pre-market Notification Details

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Correspondent

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00802526531033 P110042 000
00802526553707 P110042 000
00802526521300 P110042 000
00802526524806 P110042 000
00802526531019 P110042 000
00802526542220 P110042 009
00802526542206 P110042 009
00802526542244 P110042 009
00802526562808 P110042 017
00802526563201 P110042 017
00802526569401 P110042 033
00802526580604 P110042 043
00802526544101 P110042 043
00802526600609 P110042 043
00802526581830 P110042 043
00802526581809 P110042 043
00802526573507 P110042 043
00802526575600 P110042 043
00802526575907 P110042 043
00802526579103 P110042 043
00802526605345 P110042 058
00802526584404 P110042 058
00802526585968 P110042 058
00802526585982 P110042 058
00802526586507 P110042 058
00802526599200 P110042 077
00802526591907 P110042 102
00802526609206 P110042 123
00802526610516 P110042 123
00802526615108 P110042 132

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